Canonical Allele Identifier: CA502298297

Gene: GCGR

Linked Data

• dbSNP Id: rs1285151882
• gnomAD v2: 17-79767666-C-G
• gnomAD v4: 17-81809790-C-G
• MyVariant Identifiers: chr17:g.79767666C>G (hg19) ; chr17:g.81809790C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809790C>G , CM000679.2:g.81809790C>G	GRCh38
NC_000017.10:g.79767666C>G , CM000679.1:g.79767666C>G	GRCh37
NG_016409.1:g.8617C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.69C>G MANE Select	ENSP00000383558.3:p.Val23=
ENST00000400723.7:c.69C>G	ENSP00000383558.3:p.Val23=
ENST00000570996.5:c.69C>G	ENSP00000460976.1:p.Val23=
ENST00000572185.1:n.364C>G
ENST00000573428.1:c.69C>G	ENSP00000458930.1:p.Val23=
ENST00000574283.2:n.3C>G
NM_000160.4:c.69C>G	NP_000151.1:p.Val23=
XM_006722277.1:c.69C>G	XP_006722340.1:p.Val23=
XM_011523539.1:c.-158C>G	XP_011521841.1:n.-158C>G
XM_011523540.1:c.-448C>G	XP_011521842.1:n.-448C>G
XM_017024446.1:c.63C>G	XP_016879935.1:p.Val21=
XM_017024447.1:c.-448C>G	XP_016879936.1:n.-448C>G
NM_000160.5:c.69C>G MANE Select	NP_000151.1:p.Val23=